Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NONINVASIVE BLOOD PRESSURE MEASURE SYS

K-Number: K841103 · 1984-10-26

ApplicantPanasonic Co. Div. Matsu Elec. Corp. America
Decision Date1984-10-26
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NONINVASIVE BLOOD PRESSURE MEASURE SYS is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. It received FDA 510(k) clearance on 1984-10-26 under 510(k) number K841103. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NONINVASIVE BLOOD PRESSURE MEASURE SYS?

NONINVASIVE BLOOD PRESSURE MEASURE SYS is a medical device that received FDA 510(k) clearance on 1984-10-26. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K841103.

When did NONINVASIVE BLOOD PRESSURE MEASURE SYS receive FDA 510(k) clearance?

NONINVASIVE BLOOD PRESSURE MEASURE SYS received FDA 510(k) clearance on 1984-10-26, under 510(k) number K841103.

Who is the listed applicant for NONINVASIVE BLOOD PRESSURE MEASURE SYS?

The FDA 510(k) record lists Panasonic Co. Div. Matsu Elec. Corp. America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONINVASIVE BLOOD PRESSURE MEASURE SYS?

The FDA product code for NONINVASIVE BLOOD PRESSURE MEASURE SYS is DXN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Panasonic Co. Div. Matsu Elec. Corp. America as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K860634PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PPK832076ELECTRONIC BLOOD PRESS. METER EN-212K833510PANASONIC WH-50 HEARING AIDK832075ELECTRONIC BLOOD PRESS. METER-ZH-820PK831151PANASONIC MODEL EW-213K831150PANASONIC MODEL HV-5

View all 9 devices →

Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑